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Practical Aspects and Mechanism of Asymmetric Hydrogenation with Chiral Half-Sandwich Complexes

This review is oriented toward the asymmetric transfer hydrogenation (ATH) of imines regarding mostly fundamental, yet important topics from the practical point of view. Development of analytical methods for the monitoring of ATH (i.e., kinetics and stereoselectivity) belongs to those topics, as wel...

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Autores principales: Václavík, Jiří, Šot, Petr, Vilhanová, Beáta, Pecháček, Jan, Kuzma, Marek, Kačer, Petr
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270592/
https://www.ncbi.nlm.nih.gov/pubmed/23752467
http://dx.doi.org/10.3390/molecules18066804
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author Václavík, Jiří
Šot, Petr
Vilhanová, Beáta
Pecháček, Jan
Kuzma, Marek
Kačer, Petr
author_facet Václavík, Jiří
Šot, Petr
Vilhanová, Beáta
Pecháček, Jan
Kuzma, Marek
Kačer, Petr
author_sort Václavík, Jiří
collection PubMed
description This review is oriented toward the asymmetric transfer hydrogenation (ATH) of imines regarding mostly fundamental, yet important topics from the practical point of view. Development of analytical methods for the monitoring of ATH (i.e., kinetics and stereoselectivity) belongs to those topics, as well as studies on the influence of reaction conditions and structural variations on the reaction performance. The second part is devoted to the reaction mechanism with the emphasis on imine ATH and catalyst behaviour under acidic conditions. The review also addresses the asymmetric hydrogenation (AH) of ketones and imines using molecular hydrogen and the application of ATH in pharmaceutical projects. The contributions of our group to each area are included.
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spelling pubmed-62705922018-12-17 Practical Aspects and Mechanism of Asymmetric Hydrogenation with Chiral Half-Sandwich Complexes Václavík, Jiří Šot, Petr Vilhanová, Beáta Pecháček, Jan Kuzma, Marek Kačer, Petr Molecules Review This review is oriented toward the asymmetric transfer hydrogenation (ATH) of imines regarding mostly fundamental, yet important topics from the practical point of view. Development of analytical methods for the monitoring of ATH (i.e., kinetics and stereoselectivity) belongs to those topics, as well as studies on the influence of reaction conditions and structural variations on the reaction performance. The second part is devoted to the reaction mechanism with the emphasis on imine ATH and catalyst behaviour under acidic conditions. The review also addresses the asymmetric hydrogenation (AH) of ketones and imines using molecular hydrogen and the application of ATH in pharmaceutical projects. The contributions of our group to each area are included. MDPI 2013-06-10 /pmc/articles/PMC6270592/ /pubmed/23752467 http://dx.doi.org/10.3390/molecules18066804 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Václavík, Jiří
Šot, Petr
Vilhanová, Beáta
Pecháček, Jan
Kuzma, Marek
Kačer, Petr
Practical Aspects and Mechanism of Asymmetric Hydrogenation with Chiral Half-Sandwich Complexes
title Practical Aspects and Mechanism of Asymmetric Hydrogenation with Chiral Half-Sandwich Complexes
title_full Practical Aspects and Mechanism of Asymmetric Hydrogenation with Chiral Half-Sandwich Complexes
title_fullStr Practical Aspects and Mechanism of Asymmetric Hydrogenation with Chiral Half-Sandwich Complexes
title_full_unstemmed Practical Aspects and Mechanism of Asymmetric Hydrogenation with Chiral Half-Sandwich Complexes
title_short Practical Aspects and Mechanism of Asymmetric Hydrogenation with Chiral Half-Sandwich Complexes
title_sort practical aspects and mechanism of asymmetric hydrogenation with chiral half-sandwich complexes
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270592/
https://www.ncbi.nlm.nih.gov/pubmed/23752467
http://dx.doi.org/10.3390/molecules18066804
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